EU IVDR Training Courses on the European In Vitro Diagnostic Regulation (2017/746)

Comply Guru are the first in the world to offer Multi-Accredited European In Vitro Diagnostic Regulation (IVDR 2017/746) Training with the Regulatory Affairs Professionals Society (RAPS) and Exemplar Global offering credentials for the Medical Device Industry that are globally recognized.

The European In Vitro Diagnostic Regulation (2017/746) is the new legislation applicable to IVD medical devices being placed on the EU market. The IVDR replaces the EU In Vitro Diagnostics Directive (IVDD) 98/79/EC.

Comply Guru offer different types of EU IVDR training courses depending on the target audience and training needs. We can also tailor training to meet your company’s specific needs or requirements. Our courses are available in multiple formats from eLearning, Blended Learning or Instructor-led Learning to help you or your organization master the European In Vitro Diagnostic Regulation (IVDR 2017/746).

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EU IVDR Training for Practitioners working with the European In Vitro Diagnostic Regulation (2017/746)

4.5 ★★★★★ 71 Reviews

EU IVDR Medical Devices

EU IVDR Training for Practitioners

24hrs

Price: £895.00

EU IVDR Training for Practitioners takes you through the new European In Vitro Diagnostic Regulation (2017/746), not just from an industry perspective, but also from a Notified Body perspective. It has been specifically designed for Quality & Regulatory Professionals who are new to the Regulation.

EU IVDR Lead Auditor Training for the European In Vitro Diagnostic Regulation (2017/746)

EU IVDR Medical Devices

EU IVDR Auditor Training

20hrs

EU IVDR Auditor Training will provide learners with the knowledge and skills required to perform audits of medical device quality management systems (MD-QMS) against the European Union’s In Vitro Diagnostic Regulation (EU IVDR 2017/746) in accordance with ISO 19011 and ISO 17021 as applicable.

Person Responsible for Regulatory Compliance (PRRC) Training

4.6 ★★★★★ 17 Reviews

EU MDR EU IVDR PRRC Medical Devices

PRRC for Medical Devices

6hrs

Price: £495.00

Person Responsible for Regulatory Compliance (PRRC) Training provides clarity on the role and responsibilities of the PRRC introduced under Article 15 of the Medical Device Regulation (MDR) and In Vitro Diagnostics Regulation (IVDR).

EU IVDR Medical Devices

Advanced EU IVDR Practitioner

40hrs

Advanced EU IVDR Practitioner Training is for Quality & Regulatory Professionals who want comprehensive training on the European In Vitro Diagnostic Regulation (EU IVDR 2017/746) that is a hybrid of eLearning and Live Classes.

4.7 ★★★★★ 66 Reviews

EU IVDR Medical Devices

EU IVDR 2017/746 Essentials

2hrs

EU IVDR Essentials Training is for organizations looking for a concise, high-level introduction for their staff.

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